Canonical Allele Identifier: CA459968827
Gene: TNFRSF10A-DT HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.23225458G>C
GRCh37 chr8:g.23082971G>C
gnomAD v3:
8:23225458 G / C
gnomAD v4:
chr8-23225458-G-C
Joint Max Group AF 0.00000471 (NFE)
Genomes Max Group AF 0.00000503 (NFE)
dbSNP:
13278062
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23225458G>C , CM000670.2:g.23225458G>C GRCh38
NC_000008.10:g.23082971G>C , CM000670.1:g.23082971G>C GRCh37
NC_000008.9:g.23138916G>C NCBI36
NG_032107.1:g.4710C>G

Transcript Alleles

HGVS Amino-acid Change
NR_033928.1:n.238G>C
Search 100 bp 5'
Search 100 bp 3'